scholarly journals Correlation Between Vascular Endothelial Growth Factor (VEGF) and Ovarian Hyperstimulation Syndrome (OHSS); A Retrospective Study.

2020 ◽  
pp. 1-13

Abstract Purpose: In the context of in vitro fertilization treatment ovarian hyperstimulation syndrome can lead to a serious illness. Its pathogenesis is not fully understood, but is associated with several cytokines, enzymes and growth factors. VEGF is considered among others to be a significant factor. The aim of the present study was to investigate whether there are correlations between VEGF serum concentrations and clinical and biochemical parameters of ovarian hyperstimulation syndrome. Thus, VEGF could be used as a clinical parameter of ovarian hyperstimulation syndrome. Methods: Three patient groups were formed in which VEGF measurements were performed. In the first group, patients with ovarian hyperstimulation syndrome after stimulation treatment and hospitalization were examined. In the second group, patients with stimulation for in vitro fertilization but without OHSS were considered and in the third group, patients without stimulation treatment were recorded. The groups were comparatively statistically evaluated. Results: There was a clear association between the VEGF scores and duration of hospitalization in the diseased patients. The VEGF determinations did not differentiate between stimulated patients with and without ovarian hyperstimulation syndrome. However, there was a significant difference between stimulated and unstimulated patients. Conclusion: The determination of VEGF seems to be of limited use as a clinically useful parameter for the assessment and prognosis of ovarian hyperstimulation syndrome. Methodological weakness of the retrospective study design should be a reason for caution in interpreting the results.

2004 ◽  
Vol 89 (4) ◽  
pp. 1255-1258 ◽  
Author(s):  
Lucia Montanelli ◽  
Anne Delbaere ◽  
Costantino Di Carlo ◽  
Carmine Nappi ◽  
Guillaume Smits ◽  
...  

Abstract Ovarian hyperstimulation syndrome (OHSS) occurs mainly after excessive stimulation of the ovaries by exogenous gonadotropins administrated in the context of in vitro fertilization procedures (iatrogenic OHSS). Recently, spontaneous and recurrent occurrence of the disease (spontaneous OHSS) was shown in two families to be caused by mutations affecting the follitropin receptor (FSHr). The two mutant FSHr (T449I, D567N) harbor aminoacid substitutions in the serpentine portion of the receptor and display abnormally high sensitivity to the pregnancy hormone hCG, thus providing a satisfactory explanation to the phenotype. In addition, mutant D567N showed also increased sensitivity to thyrotopin (TSH) and displayed increase in basal (ligand-independent) activity. In this report, we describe a new familial case of recurrent OHSS. The affected women were heterozygous for a different mutation involving codon 449, where an alanine was substituted for threonine. Similar to D567N, the T449A FSHr mutant shows an increase of its sensitivity to both hCG and TSH, together with an increase in basal activity. Together with the two previous studies, this report shows that inappropriate stimulation of the FSHr by hCG is a cause of spontaneous OHSS.


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